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Gene therapy for sickle cell disease
BACKGROUND: Sickle cell disease encompasses a group of genetic disorders characterized by the presence of at least one hemoglobin S (Hb S) allele, and a second abnormal allele that could allow abnormal hemoglobin polymerisation leading to a symptomatic disorder. Autosomal recessive disorders (such a...
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| Publicat a: | Cochrane Database Syst Rev |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley & Sons, Ltd
2018
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6517046/ https://ncbi.nlm.nih.gov/pubmed/30480767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD007652.pub6 |
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